PlainRecalls
FDA Devices Moderate Class II Ongoing

Integra Universal Flexible Arm part number REF 1362275

Reported: April 20, 2022 Initiated: February 28, 2022 #Z-0906-2022

Product Description

Integra Universal Flexible Arm part number REF 1362275

Reason for Recall

Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.

Details

Units Affected
54
Distribution
US Nationwide Distribution: AL, AZ, FL, GA, IL, MA, MD, NY, OH, OR, PA, TX
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
Integra Universal Flexible Arm part number REF 1362275. Recalled by Integra LifeSciences Corp.. Units affected: 54.
Why was this product recalled?
Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 20, 2022. Severity: Moderate. Recall number: Z-0906-2022.